Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:21031586-21031697 | Common:1; Rare:49 | ||||
chr9:21994344-21994373 | Rare:9; Clinvar:1; Clinvar (benign):2 | ||||
chr9:21994375-21994686 | Common:1; Rare:89; Clinvar (benign):1 | ||||
chr9:26892738-26892895 | Common:1; Rare:77 | ||||
chr9:26947146-26947306 | Rare:53 | ||||
chr9:26956255-26956470 | Common:2; Rare:80 | ||||
chr9:32384514-32384721 | Common:1; Rare:79 | ||||
chr9:32573053-32573321 | Common:4; Rare:94 | ||||
chr9:33001543-33001757 | Common:3; Rare:104; Clinvar (benign):4 | ||||
chr9:33025083-33025383 | Common:7; Rare:124 | ||||
chr9:33166890-33166956 | Rare:28 | ||||
chr9:33167322-33167563 | Rare:93 | ||||
chr9:33290265-33290563 | Common:2; Rare:102 | ||||
chr9:33473838-33474143 | Common:4; Rare:94 | ||||
chr9:34048876-34049014 | Common:1; Rare:55 |